HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine, hexahydrate → HCID 21517974, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine, hexahydrate | HCID 120181 | — |
| Reactant | 4-(2-Chloro-6-methyl-5-nitro-4-pyrimidinyl)morpholine | HCID 7147283 | — |
| Solvent | HCID 22407776 | HCID 22407776 | — |
| Product | HCID 21517974 | HCID 21517974 | — |
Reaction Steps
A solution of 2.6 gm (0.01 mol) of 2-chloro-6-methyl-4-morpholino-5-nitro-pyrimidine (m.p. 127°-129°C, prepared from 2,4-dichloro-6-methyl-5-nitro-pyrimidine and morpholine) in 100 ml of acetone/dioxane (1:1) was added dropwise, while stirring and cooling, to a solution of 19.4 gm (0.1 mol) of piperazine hexahydrate in 300 ml of acetone/dioxane (1:1) at about 5°C. After about 1 hour the solvents were distilled off in vacuo, and the residue was taken up in about 100 ml of water. The insoluble reaction product was suction-filtered off, washed with water and dried. Yield: 3.0 gm (97% of theory). After one reprecipitation from about 0.2 N hydrochloric acid with 2 N ammonia, the reaction product of the formula ##SPC5##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03975384 |
| Source dataset | uspto-grants-1976_08 |
| ORD ID | ord-6e4c6b7ec1ca45e99ab18071691ca9e6 |
| Source note | uspto-grants-1976_08 |